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Re: stocknewbie312 post# 170017

Tuesday, 01/23/2024 4:00:18 PM

Tuesday, January 23, 2024 4:00:18 PM

Post# of 174380
Great question...I have no clue. Just sitting here I wouldn't think it is required - I think in the IDE submission we just need to provide enough data to the FDA to prove this technology is safe enough to conduct trials on humans but perhaps the testing protocol with Mayo approval is a helpful plus in our IDE? Maybe someone else can provide a more solid answer to a good question...anyone...Bueller?
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